rs28897759
|
|
|
0.810 |
GeneticVariation |
BEFREE |
We analyzed a missense VUS located in BRCA2 (p.Asn3124Ile; HGVS: BRCA2 c.9371A > T) present in seven independent high-risk breast cancer families that were counseled and genetically tested in South-West Germany.
|
24728577 |
2014 |
rs28897759
|
|
T |
0.810 |
GeneticVariation |
CLINVAR |
|
|
|
rs28897759
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
|
|
|
rs41293511
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Risk assessment, genetic counseling, and genetic testing for BRCA-related cancer in women: U.S. Preventive Services Task Force recommendation statement.
|
24366376 |
2014 |
rs41293511
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Summaries for patients. Assessing the genetic risk for BRCA-related breast or ovarian cancer in women: recommendations from the U.S. Preventive Services Task Force.
|
24366402 |
2014 |
rs45580035
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Summaries for patients. Assessing the genetic risk for BRCA-related breast or ovarian cancer in women: recommendations from the U.S. Preventive Services Task Force.
|
24366402 |
2014 |
rs45580035
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Risk assessment, genetic counseling, and genetic testing for BRCA-related cancer in women: U.S. Preventive Services Task Force recommendation statement.
|
24366376 |
2014 |
rs41293511
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
The emerging landscape of breast cancer susceptibility.
|
18163131 |
2008 |
rs45580035
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
The emerging landscape of breast cancer susceptibility.
|
18163131 |
2008 |
rs41293511
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Risk assessment and genetic counseling for hereditary breast and ovarian cancer: recommendations of the National Society of Genetic Counselors.
|
17508274 |
2007 |
rs45580035
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Risk assessment and genetic counseling for hereditary breast and ovarian cancer: recommendations of the National Society of Genetic Counselors.
|
17508274 |
2007 |
rs45580035
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Control of BRCA2 cellular and clinical functions by a nuclear partner, PALB2.
|
16793542 |
2006 |
rs41293511
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors.
|
15604628 |
2004 |
rs45580035
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors.
|
15604628 |
2004 |
rs45580035
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
BRCA1 and BRCA2 germline mutation spectrum and frequencies in Belgian breast/ovarian cancer families.
|
15026808 |
2004 |
rs45580035
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel germline mutations in the BRCA1 and BRCA2 genes in Indian breast and breast-ovarian cancer families.
|
14722926 |
2004 |
rs45580035
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
BRCA1 and BRCA2 germline mutations in Korean patients with sporadic breast cancer.
|
15365993 |
2004 |
rs45580035
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Hereditary breast and ovarian cancer in Cyprus: identification of a founder BRCA2 mutation.
|
15172753 |
2004 |
rs45580035
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
BRCA2 germline mutations in familial pancreatic carcinoma.
|
12569143 |
2003 |
rs45580035
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Twenty-three novel BRCA1 and BRCA2 sequence alterations in breast and/or ovarian cancer families in Southern Germany.
|
12938098 |
2003 |
rs45580035
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
BRCA2 gene mutations in families with aggregations of breast and stomach cancers.
|
12373604 |
2002 |
rs45580035
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Somatic mutations in the BRCA2 gene and high frequency of allelic loss of BRCA2 in sporadic male breast cancer.
|
11948477 |
2002 |
rs45580035
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
BRCA1 and BRCA2 sequence variants in Chinese breast cancer families.
|
12442274 |
2002 |
rs45580035
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
BRCA2 T2722R is a deleterious allele that causes exon skipping.
|
12145750 |
2002 |
rs45580035
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
An improved high throughput heteroduplex mutation detection system for screening BRCA2 mutations-fluorescent mutation detection (F-MD).
|
11241844 |
2001 |